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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795383Generated: November 3, 2026

3-Chloro-2,5-dimethylpyrazine → 2,5-Dimethyl-3-phenylpyrazine

https://huagongshe.com/reaction/1795383

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2,5-dimethylpyrazineHCID 66771—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Product2,5-Dimethyl-3-phenylpyrazineHCID 1364292064.4%

Reaction Steps

A solution of phenylmagnesium bromide (1M in THF, 5.6 mL, 5.6 mmol) is added to a solution of 3-chloro-2,5-dimethylpyrazine (346 mg, 2.42 mmol) and Fe(acac)3 (43 mg, 0.12 mmol) in THF (10 mL) at −30° C. After stirring for 30 min at that temperature, the reaction is quenched with brine, the aqueous layer is extracted with Et2O, the combined organic phases are dried over Na2SO4 and evaporated, and the residue is purified by flash chromatography (hexane/ethyl acetate, 10:1). After eluting a first fraction containing biphenyl (212 mg), one obtains 2,5-dimethyl-3-phenylpyrazine as a pale yellow syrup (287 mg, 64%). 1H NMR (300 MHz, CD2Cl2) δ 8.31 (s, 1H), 7.55–7.59 (m, 2H), 7.43–7.51 (m, 3H), 2.55 (s, 3H), 2.54 (s, 3H). 13C NMR (75 MHz, CD2Cl2) δ 152.7, 150.6, 148.4, 142.1, 139.5, 129.3, 128.7, 128.6, 22.7, 21.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026478B2
Source datasetuspto-grants-2006_04
ORD IDord-af417605eafc4f64b6c1d1a370bd2027
Source noteuspto-grants-2006_04